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Triple Antibiotic - 11822-0679-1 - (Bacitracin, Neomycin, Polymyxin B, Pramoxine HCl)

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Drug Information of Triple Antibiotic

Product NDC: 11822-0679
Proprietary Name: Triple Antibiotic
Non Proprietary Name: Bacitracin, Neomycin, Polymyxin B, Pramoxine HCl
Active Ingredient(s): 500; 3.5; 10000; 10    [USP'U]/g; mg/g; [USP'U]/g; mg/g & nbsp;   Bacitracin, Neomycin, Polymyxin B, Pramoxine HCl
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Triple Antibiotic

Product NDC: 11822-0679
Labeler Name: Rite Aid Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20050817

Package Information of Triple Antibiotic

Package NDC: 11822-0679-1
Package Description: 1 TUBE in 1 CARTON (11822-0679-1) > 14 g in 1 TUBE

NDC Information of Triple Antibiotic

NDC Code 11822-0679-1
Proprietary Name Triple Antibiotic
Package Description 1 TUBE in 1 CARTON (11822-0679-1) > 14 g in 1 TUBE
Product NDC 11822-0679
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Bacitracin, Neomycin, Polymyxin B, Pramoxine HCl
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20050817
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Rite Aid Corporation
Substance Name BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE
Strength Number 500; 3.5; 10000; 10
Strength Unit [USP'U]/g; mg/g; [USP'U]/g; mg/g
Pharmaceutical Classes

Complete Information of Triple Antibiotic


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